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REACH - Registration, Evaluation and Authorisation of Chemicals
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REACH - Registration, Evaluation and Authorisation of Chemicals
TITLE-II
: REGISTRATION OF SUBSTANCES
CHAPTER-3
: Obligation to register and information requirements for certain types of isolated intermediates
ARTICLE 17
:
Registration
of
on-site isolated intermediates
ARTICLE 17:
Registration
of
on-site isolated intermediates
1. Any
manufacturer
of an
on-site isolated intermediate
in
quantities
of 1 tonne or more per
year
shall submit a
registration
to the
Agency
for the
on-site isolated intermediate
.
2. A
registration
for an
on-site isolated intermediate
shall
include
all the following
information
, to the
extent
that the
manufacturer
is able to submit it without any additional
testing
:
(a) the
identity
of the
manufacturer
as specified in section 1 of Annex VI;
(b) the
identity
of the
intermediate
as specified in sections 2.1 to 2.3.4 of Annex VI;
(c) the
classification
of the
intermediate
as specified in section 4 of Annex VI;
(d) any available
existing
information
on physicochemical,
human health
or
environmental
properties of the
intermediate
. Where a
full study report
is available, a
study
summary
shall be submitted;
(e) a brief
general
description
of the use, as specified in section 3.5 of Annex VI; (f)
details
of the
risk management
measures
applied.
Except in
cases
covered under
Article
25
(3),
Article
27
(6) or
Article
30
(3), the
registrant
shall be in
legitimate
possession
of or have
permission
to refer to the
full study report
summarised under (d) for the
purpose
of
registration
. The
registration
shall be accompanied by the
fee
required in
accordance
with Title IX.
3. Paragraph 2 shall apply only to
on-site isolated intermediates
if the
manufacturer
confirms that the
substance
is only
manufactured
and used under strictly controlled
conditions
in that it is rigorously contained by
technical
means during its whole lifecycle.
Control
and procedural
technologies
shall be used to minimise
emission
and any resulting
exposure
. If these
conditions
are not fulfilled, the
registration
shall
include
the
information
specified in
Article
10
.
[
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]
Referred by:
ARTICLE 6
:
General obligation
to
register
substances
on their own or in
preparations
ARTICLE 9
:
Exemption
from the
general obligation
to
register
for
product
and process orientated
research
and
development
(PPORD)
ARTICLE 19
:
Joint
submission of
data
on isolated
intermediates
by multiple
registrants
ARTICLE 20
:
Duties
of the
Agency
ARTICLE 23
:
Specific provisions
for
phase-in substances
ARTICLE 74
:
Fees
and
charges